A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14367442



Internal ID22270822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26281566..26281566hg38UCSC Ensembl
chr13:26855703..26855703hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559940
Supporting Variants
SamplesNA19239
Known GenesCDK8
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14367442
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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